I am not aware of a particular diet for people with ataxia recommended by Ataxia UK, other than a gluten free diet for people with gluten ataxia. Is this the diet you are referring to?
Hi Paul apart from the strict diet I hope you are well. The long haired general (wife) has past comment that I should consider a change in diet but I’m holding out at moment as I anticipate I will be but on a strict gluten free diet on my next visit to Sheffield as TG6 antibodies were found. I like a biscuit with my brew so I’m gonna stick with that for now. But could do with shedding a few pounds 🤨 take care friend
This diet is a complete change for me so I suppose it will take some getting used to but if it makes a difference for the better it will be worth it. See what is advised on your next appointment and of course what the long haired general is happy with 😊.
All my close family turned into Neurologists 3 weeks after I was diagnosed 🥴
Hi Paul on the discovery of the TG6 antibodies I was informed not to change my diet ☺️until further blood tests and MRI spectroscopy was done at moment I’m using this as a defense tactic against the general but i fear I will have no choice but to change this tactic. I anticipate a gluten free diet will be advised and I will give that my best because joking aside I’m in my chin strap with some of the new symptoms.
Keep at the diet friend if it’s going to help we need all we can get and let’s face it the wives know what is best for us.
This diet was found from the National Ataxia Foundation (USA) it’s a mixture of high vibre and vitamins. I’ve had some success with more energy and feeling better in myself although I don’t follow it to the letter I was always hungry 😊
I’m a bit concerned that you won’t be able to recognise me on our top secret Saturday nights out so I’ll have my yellow suit green tie and red shoes on, it’s called the traffic light look 👍🏻😂
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